DOI: 10.1055/s-00000071

Seminars in Neurology

References

Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK.
NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).

Am J Hum Genet 2003;
73 (4) 967-971

Download Bibliographical Data

Search in:
Access: